Variant report

Variant	nsv832110
Chromosome Location	chr11:33329586-33497555
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1643)
CpG islands
(count:1159)
Chromatin interactive
region (count:121)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:1643 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33351286-33351649	K562	blood:	n/a	n/a
3	ARID3A	chr11:33383925-33384254	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:33364523-33364723	K562	blood:	n/a	n/a
5	ARID3A	chr11:33383912-33384198	K562	blood:	n/a	n/a
6	ARID3A	chr11:33342559-33342940	K562	blood:	n/a	n/a
7	ARID3A	chr11:33351288-33351628	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:33394101-33394301	HepG2	liver:	n/a	n/a
9	ATF1	chr11:33394198-33394335	K562	blood:	n/a	n/a
10	ATF1	chr11:33351332-33351614	K562	blood:	n/a	n/a
11	ATF1	chr11:33329665-33330069	K562	blood:	n/a	n/a
12	ATF1	chr11:33342458-33342912	K562	blood:	n/a	n/a
13	ATF1	chr11:33341606-33341888	K562	blood:	n/a	n/a
14	ATF2	chr11:33411036-33411671	GM12878	blood:	n/a	n/a
15	ATF2	chr11:33404441-33405009	GM12878	blood:	n/a	n/a
16	ATF2	chr11:33409013-33410089	GM12878	blood:	n/a	n/a
17	ATF2	chr11:33404542-33405049	GM12878	blood:	n/a	n/a
18	ATF2	chr11:33409042-33410013	GM12878	blood:	n/a	n/a
19	ATF3	chr11:33342449-33342699	K562	blood:	n/a	n/a
20	ATF3	chr11:33382233-33382453	K562	blood:	n/a	chr11:33382358-33382372
21	BACH1	chr11:33364471-33364818	K562	blood:	n/a	n/a
22	BACH1	chr11:33397385-33398563	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr11:33363592-33363812	GM12878	blood:	n/a	n/a
24	BATF	chr11:33404575-33404911	GM12878	blood:	n/a	n/a
25	BATF	chr11:33408990-33409983	GM12878	blood:	n/a	n/a
26	BATF	chr11:33363521-33363808	GM12878	blood:	n/a	n/a
27	BATF	chr11:33411172-33411511	GM12878	blood:	n/a	n/a
28	BATF	chr11:33404521-33404947	GM12878	blood:	n/a	n/a
29	BATF	chr11:33409566-33409855	GM12878	blood:	n/a	n/a
30	BCL11A	chr11:33409034-33409543	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:33409556-33409888	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:33404557-33404945	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:33409572-33409836	GM12878	blood:	n/a	n/a
34	BCL3	chr11:33404619-33404913	GM12878	blood:	n/a	n/a
35	BCL3	chr11:33409282-33409904	GM12878	blood:	n/a	n/a
36	BCLAF1	chr11:33341910-33342551	GM12878	blood:	n/a	n/a
37	BCLAF1	chr11:33404519-33404990	GM12878	blood:	n/a	n/a
38	BCLAF1	chr11:33409067-33410001	GM12878	blood:	n/a	n/a
39	BCLAF1	chr11:33409061-33410037	GM12878	blood:	n/a	n/a
40	BHLHE40	chr11:33401529-33401825	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:33427892-33427983	K562	blood:	n/a	n/a
42	BHLHE40	chr11:33342530-33342916	K562	blood:	n/a	n/a
43	BHLHE40	chr11:33484666-33484886	K562	blood:	n/a	n/a
44	BHLHE40	chr11:33404539-33405771	GM12878	blood:	n/a	n/a
45	BHLHE40	chr11:33369101-33369338	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:33345920-33346220	GM12878	blood:	n/a	n/a
47	BRCA1	chr11:33337746-33337909	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:33425244-33425411	IMR90	lung:	n/a	n/a
49	CEBPB	chr11:33342449-33342823	K562	blood:	n/a	n/a
50	CEBPB	chr11:33382242-33382528	A549	lung:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33396983-33397033	HCF	heart:	n/a
2	chr11:33346306-33346356	K562	blood:	n/a
3	chr11:33397821-33397871	K562	blood:	n/a
4	chr11:33396859-33396909	AG09319	gingival:	n/a
5	chr11:33397689-33397739	ECC-1	luminal epithelium:	n/a
6	chr11:33398245-33398295	NHDF-neo	bronchial:	n/a
7	chr11:33375412-33375462	Hepatocyte	liver:	n/a
8	chr11:33399978-33400028	MCF-7	breast:	n/a
9	chr11:33398173-33398223	NH-A	brain:	n/a
10	chr11:33442321-33442371	AG09319	gingival:	n/a
11	chr11:33397679-33397729	T-47D	breast:	n/a
12	chr11:33397387-33397437	Hela-S3	cervix:	n/a
13	chr11:33394273-33394323	NB4	blood:	n/a
14	chr11:33334443-33334493	NHBE	bronchial:	n/a
15	chr11:33346306-33346356	GM12892	blood:	n/a
16	chr11:33334443-33334493	HUVEC	blood vessel:	n/a
17	chr11:33396983-33397033	IMR90	lung:	fetal
18	chr11:33394273-33394323	NHDF-neo	bronchial:	n/a
19	chr11:33398173-33398223	HRCEpiC	kidney:	n/a
20	chr11:33442321-33442371	K562	blood:	n/a
21	chr11:33453389-33453439	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:33397689-33397739	IMR90	lung:	fetal
23	chr11:33398366-33398416	AG10803	skin:	n/a
24	chr11:33474484-33474534	HCM	heart:	n/a
25	chr11:33398173-33398223	K562	blood:	n/a
26	chr11:33396983-33397033	H1-hESC	embryonic stem cell:	embryo
27	chr11:33442321-33442371	HAEpiC	amniotic membrane:	n/a
28	chr11:33394273-33394323	HCT-116	colon:	n/a
29	chr11:33397821-33397871	HepG2	liver:	n/a
30	chr11:33396859-33396909	A549	lung:	n/a
31	chr11:33396983-33397033	HCT-116	colon:	n/a
32	chr11:33398245-33398295	MCF-7	breast:	n/a
33	chr11:33442321-33442371	HMEC	breast:	n/a
34	chr11:33399978-33400028	SKMC	muscle:	n/a
35	chr11:33397679-33397729	GM12892	blood:	n/a
36	chr11:33399978-33400028	ovcar-3	ovarian:	n/a
37	chr11:33398173-33398223	MCF10A-Er-Src	breast:	n/a
38	chr11:33396859-33396909	MCF-7	breast:	n/a
39	chr11:33399978-33400028	SK-N-MC	brain:	n/a
40	chr11:33398366-33398416	HEK293	kidney:	embryo
41	chr11:33396859-33396909	HEK293	kidney:	embryo
42	chr11:33396983-33397033	NHBE	bronchial:	n/a
43	chr11:33334443-33334493	AG09319	gingival:	n/a
44	chr11:33396983-33397033	Hepatocyte	liver:	n/a
45	chr11:33346306-33346356	NH-A	brain:	n/a
46	chr11:33474484-33474534	H1-hESC	embryonic stem cell:	embryo
47	chr11:33346306-33346356	ProgFib	skin:	n/a
48	chr11:33397387-33397437	GM12892	blood:	n/a
49	chr11:33442321-33442371	HRCEpiC	kidney:	n/a
50	chr11:33396983-33397033	HNPCEpiC	eye:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:33365715..33367217-chr11:33368914..33370934,2	K562	blood:
2	chr11:33382588..33385319-chr11:33707872..33709435,2	MCF-7	breast:
3	chr11:33392077..33394205-chr11:33397342..33400084,3	K562	blood:
4	chr11:33278606..33279290-chr11:33341646..33342645,2	MCF-7	breast:
5	chr11:33340003..33342699-chr11:33347574..33349225,2	K562	blood:
6	chr11:33345699..33348337-chr11:33348377..33350579,2	K562	blood:
7	chr11:33278813..33281447-chr11:33356120..33358697,4	MCF-7	breast:
8	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
9	chr11:33278004..33279582-chr11:33355016..33356972,2	MCF-7	breast:
10	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
11	chr11:33340003..33342699-chr11:33347574..33349225,2	K562	blood:
12	chr11:33278126..33279710-chr11:33347501..33349004,2	MCF-7	breast:
13	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
14	chr11:33187508..33188019-chr11:33392733..33393351,2	MCF-7	breast:
15	chr11:33370166..33372800-chr11:33374328..33376444,2	MCF-7	breast:
16	chr11:33350757..33353405-chr11:33354429..33357042,2	K562	blood:
17	chr11:33404576..33406306-chr11:33408202..33410856,2	MCF-7	breast:
18	chr11:33391648..33394205-chr11:33396367..33400084,3	K562	blood:
19	chr11:33343171..33345414-chr11:33349512..33351209,2	K562	blood:
20	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
21	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
22	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
23	chr11:33422636..33425023-chr11:33427111..33429775,2	MCF-7	breast:
24	chr11:33330031..33332498-chr11:33332591..33335075,2	MCF-7	breast:
25	chr11:33399022..33400859-chr11:33402110..33404984,2	K562	blood:
26	chr11:33327923..33330739-chr11:33334207..33336221,2	K562	blood:
27	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
28	chr11:33366273..33368343-chr11:33370196..33371959,2	K562	blood:
29	chr11:33416676..33419367-chr11:33423190..33425357,2	K562	blood:
30	chr11:33330605..33333745-chr11:33333939..33336380,3	K562	blood:
31	chr11:33351340..33351943-chr11:33383658..33384527,2	K562	blood:
32	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
33	chr11:33428202..33430119-chr11:33432481..33434506,2	MCF-7	breast:
34	chr11:33383578..33384538-chr11:33708929..33709708,5	K562	blood:
35	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
36	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
37	chr11:33187513..33188468-chr11:33351019..33351906,6	K562	blood:
38	chr11:33380757..33382861-chr11:33395684..33398398,2	MCF-7	breast:
39	chr11:33366360..33368007-chr11:33376347..33377878,2	K562	blood:
40	chr11:33308929..33311681-chr11:33352469..33354383,2	MCF-7	breast:
41	chr11:33276714..33280349-chr11:33350703..33354404,4	MCF-7	breast:
42	chr11:33326071..33328703-chr11:33331126..33332666,2	K562	blood:
43	chr11:33450480..33453431-chr11:33470843..33473158,2	MCF-7	breast:
44	chr11:33278689..33280532-chr11:33344460..33346639,2	K562	blood:
45	chr11:33353025..33355412-chr11:33355874..33357955,2	MCF-7	breast:
46	chr11:32982327..32984023-chr11:33390393..33392493,2	K562	blood:
47	chr11:33347406..33349145-chr11:33350262..33352793,2	MCF-7	breast:
48	chr11:33183085..33184714-chr11:33357286..33359018,2	K562	blood:
49	chr11:33351340..33351943-chr11:33383658..33384527,2	K562	blood:
50	chr11:33277371..33280516-chr11:33349638..33353162,5	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11L1-4	chr11:33334713-33335041	expReg_chr11_2985_+
2	lnc-TCP11L1-3	chr11:33333205-33333598	expReg_chr11_2971_+
3	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701
4	lnc-HIPK3-2	chr11:33424762-33425151	NONHSAT018700

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HIPK3	hsa-miR-124-3p	chr11:33375663-33375670
2	HIPK3	hsa-miR-20b-5p	chr11:33375245-33375267
3	HIPK3	hsa-miR-19b-3p	chr11:33375260-33375282
4	HIPK3	hsa-miR-92a-3p	chr11:33375228-33375234
5	HIPK3	hsa-miR-19b-3p	chr11:33358682-33358704
6	HIPK3	hsa-miR-20b-5p	chr11:33375709-33375730
7	HIPK3	hsa-miR-124-3p	chr11:33375651-33375670
8	HIPK3	hsa-miR-106a-5p	chr11:33375709-33375730
9	HIPK3	hsa-miR-19b-3p	chr11:33375275-33375282
10	HIPK3	hsa-miR-124-3p	chr11:33375376-33375395
11	HIPK3	hsa-miR-106a-5p	chr11:33375245-33375267
12	HIPK3	hsa-miR-92a-3p	chr11:33375214-33375235
13	HIPK3	hsa-miR-92a-3p	chr11:33375388-33375409
14	HIPK3	hsa-miR-335-5p	chr11:33375589-33375614

Variant related genes	Relation type
ENSG00000255207	TF binding region
HIPK3	TF binding region
ENSG00000254537	TF binding region
ENSG00000223134	TF binding region
ENSG00000255207	CpG island
HIPK3	CpG island
ENSG00000254537	CpG island
ENSG00000223134	CpG island
ENSG00000110422	chromatin interactions
ENSG00000254537	chromatin interactions
ENSG00000255207	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000223134	chromatin interactions
ENSG00000206808	chromatin interactions

Extended variants
information (count: 6235 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6235 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538996248	chr11:33329631-33329632	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs534169013	chr11:33329656-33329657	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs35563688	chr11:33329684-33329685	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs563088537	chr11:33329693-33329694	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs144614644	chr11:33329711-33329712	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs531924867	chr11:33329738-33329739	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs190493438	chr11:33329792-33329793	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs376146338	chr11:33329839-33329840	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs558728017	chr11:33329879-33329880	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs529732093	chr11:33329888-33329889	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs570167466	chr11:33329902-33329903	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs532885812	chr11:33329939-33329940	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs571068413	chr11:33329945-33329946	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs546322785	chr11:33329960-33329961	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs557299361	chr11:33329995-33329996	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140996650	chr11:33330002-33330003	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs193121205	chr11:33330022-33330023	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555625922	chr11:33330085-33330086	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs569063092	chr11:33330090-33330091	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs570672400	chr11:33330132-33330133	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs537995154	chr11:33330157-33330158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558004127	chr11:33330159-33330160	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs578117103	chr11:33330161-33330162	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs72216768	chr11:33330178-33330179	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs35281619	chr11:33330188-33330189	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs538354135	chr11:33330189-33330190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs540717931	chr11:33330260-33330261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35729613	chr11:33330288-33330289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs397945836	chr11:33330303-33330304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554336574	chr11:33330314-33330315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573978234	chr11:33330318-33330319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201385398	chr11:33330353-33330354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542699603	chr11:33330376-33330377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563157218	chr11:33330476-33330477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372704468	chr11:33330496-33330497	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546247358	chr11:33330512-33330513	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185092572	chr11:33330549-33330550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546441578	chr11:33330597-33330598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116011221	chr11:33330775-33330776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs565154503	chr11:33330810-33330811	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs527907062	chr11:33330812-33330813	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189952965	chr11:33330815-33330816	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566486820	chr11:33330818-33330819	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528840349	chr11:33330831-33330832	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548702946	chr11:33330924-33330925	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181752203	chr11:33331011-33331012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538151561	chr11:33331106-33331107	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551732685	chr11:33331109-33331110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs571447303	chr11:33331124-33331125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556354360	chr11:33331152-33331153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2720 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33290000-33336800	Weak transcription	Lung	lung
2	chr11:33296400-33332200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:33298800-33339000	Weak transcription	NHEK	skin
4	chr11:33299400-33331200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr11:33302200-33333400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:33308600-33331400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr11:33308800-33329600	Weak transcription	HUVEC	blood vessel
8	chr11:33309000-33331800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr11:33309000-33332200	Weak transcription	Fetal Thymus	thymus
10	chr11:33309000-33339000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:33309600-33332200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr11:33310800-33334400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr11:33311000-33329600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr11:33313200-33329600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:33313200-33332600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr11:33313400-33333200	Weak transcription	Aorta	Aorta
17	chr11:33314400-33331200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr11:33316600-33335400	Weak transcription	Esophagus	oesophagus
19	chr11:33317200-33329600	Weak transcription	NHLF	lung
20	chr11:33317200-33340600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr11:33317400-33330800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr11:33317400-33331000	Weak transcription	Small Intestine	intestine
23	chr11:33317400-33332800	Weak transcription	Pancreas	Pancrea
24	chr11:33317400-33336800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr11:33317400-33337200	Weak transcription	Duodenum Mucosa	Duodenum
26	chr11:33317400-33345800	Weak transcription	Gastric	stomach
27	chr11:33318000-33329600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr11:33318000-33360200	Weak transcription	Primary T cells from cord blood	blood
29	chr11:33318400-33329600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr11:33318400-33329600	Weak transcription	HSMM	muscle
31	chr11:33318400-33333000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr11:33318400-33335400	Weak transcription	Ovary	ovary
33	chr11:33318600-33338200	Weak transcription	Fetal Muscle Trunk	muscle
34	chr11:33319200-33335000	Weak transcription	Fetal Lung	lung
35	chr11:33319200-33348800	Weak transcription	Hela-S3	cervix
36	chr11:33319600-33332000	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr11:33319800-33330800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:33319800-33332400	Weak transcription	Fetal Intestine Small	intestine
39	chr11:33319800-33342800	Weak transcription	Fetal Intestine Large	intestine
40	chr11:33319800-33352600	Weak transcription	Dnd41	blood
41	chr11:33320000-33330800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr11:33320000-33332200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr11:33320200-33331800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:33320200-33332400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:33320400-33332200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:33320400-33338800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:33320400-33340400	Weak transcription	Primary hematopoietic stem cells	blood
48	chr11:33320400-33341600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:33320400-33341800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr11:33320600-33329600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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